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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094478copy number variation1nstd102humanUncertain significance GRCh37 chr13: 48,615,046-48,930,735 , GRCh38.p12 chr13: 48,040,910-48,356,599 RB1, PCNPP5, 8 more genes
    nsv7074086inversion1nstd229human GRCh38 chr13: 47,957,386-48,970,527 , GRCh37.p13 chr13: 48,531,521-49,544,663 SUCLA2, PPP1R26P1, 17 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7068022inversion1nstd229human GRCh38 chr13: 48,051,653-48,055,971 , GRCh37.p13 chr13: 48,625,789-48,630,107 NUDT15
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6942711copy number variation1nstd229human GRCh38 chr13: 47,954,978-51,016,028 , GRCh37.p13 chr13: 48,529,113-51,590,164 COX7CP1, CTAGE10P, 60 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6309510copy number variation1nstd102humanPathogenic GRCh37 chr13: 48,611,883-48,878,195 , GRCh38.p12 chr13: 48,037,747-48,304,059 RB1, ITM2B, 6 more genes
    nsv6309509copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr13: 48,517,506-49,070,513 , GRCh38.p12 chr13: 47,943,371-48,496,377 POLR2KP2, LOC105370198, 12 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6133097copy number variation1nstd213human GRCh37 chr13: 47,920,000-48,790,001 , GRCh38.p12 chr13: 47,345,865-48,215,865 SUCLA2, MED4, 10 more genes
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132557copy number variation1nstd213human GRCh37 chr13: 44,840,000-52,410,001 , GRCh38.p12 chr13: 44,265,864-51,835,865 , RCBTB2, 160 more genes
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